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Research 691–720 of 1000+
- Keratosis follicularis spinulosa decalvans in a female
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS
- Androgenetic Alopecia in Al-Qalyubia Governorate: A Comprehensive Review
- This month in JAAD Case Reports: October 2023—Central centrifugal cicatricial alopecia in Black men
- Androgenetic alopecia: pathogenesis and potential for therapy
- Melanocytes: The new Black
- Goat Genomic Resources: The Search for Genes Associated with Its Economic Traits
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Inherited Disorders of the Hair
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Hereditary Chorea Associated With and Aggravated by Systemic Lupus Erythematosus
- Influence of Scalp Problems on Physical Properties of Hair and Their Prevention by Plant Extracts
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- EXPLORATION OF THE MAHIYAT-E- MARAḌI (ETIOPATHOGENESIS) OF AMRĀḌ-E-SHA’R (HAIR DISORDERS) IN UNANI MEDICINE: A SYSTEMATIC LITERATURE REVIEW
- Post‐finasteride syndrome: real or myth?
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Pigmentary mosaicism: An update
- Woodhouse-Sakati syndrome (WSS)
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- A Mosaic Hotspot <i>PLCD1</i> Variant, Detectable in Blood‐Derived DNA, Associated With Nevus Trichilemmocysticus
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Alopecia androgénica femenina: nuevos factores fisiopatológicos y futuras tendencias para un abordaje clínico más integral
- The Skin at Different Ages
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Hair shaft disorders
- Endocrine Influences on Hair Growth